Real time PCR assays to detect mutations in the biotinidase gene for newborn screening

ABSTRACT

Biotinidase deficiency is detected by determining the activity of the biotinidase enzyme utilizing a newborn dried blood spot and calorimetric end point analysis. The four mutations most commonly associated with complete biotinidase deficiency are G98: d7i3, Q456H, R538C, and the double mutation D444H:A171T. Partial biotinidase deficiency is almost universally attributed to the D444H mutation. To more effectively distinguish between profound and partial biotinidase deficiency, a panel of assays utilizing real time PCR and melting curve analysis is developed to detect those mutations listed above. In newborn screening for biotinidase deficiency, the analysis of common mutations is useful to distinguish between partial and complete enzyme deficiency. Combining biotinidase enzyme analysis with genotypic data also increases the sensitivity of screening for biotinidase deficiency and provides information useful to clinicians earlier than would otherwise be possible.

SPECIFIC REFERENCE

[0001] The present application claims benefit of provisional application Ser. No. 60/400264, filed Aug. 1, 2002.

BACKGROUND

[0002] 1. Description of the Related Art

[0003] Biotinidase deficiency is an autosomal recessive metabolic disorder occurring in 1:80,000 live births. Those affected by biotinidase deficiency exhibit irreversible neurological problems, seizures, developmental delays, hypotonia, ataxia, cutaneous and other symptoms. Symptoms are preventable and in some cases reversible through oral biotin supplementation. Prospective newborn screening for biotinidase deficiency is, therefore, performed in much of the USA and in numerous other countries. Biotinidase deficiency results from mutations in the biotinidase gene and depending upon the nature of the mutation(s), the enzyme deficiency may be either complete or partial. Mean biotinidase activity is 7.1 nmol/min/ml serum in normal newborns. Those affected with complete biotinidase deficiency have enzymes that produce <10% of mean normal activity, while those affected with partial deficiency have enzymes that produce 10-30% of normal activity.

[0004] In newborn screening laboratories, assaying for biotinidase deficiency is performed using an extract of whole blood derived from the universally collected newborn dried blood spot (DBS). Whole blood extracted from a DBS specimen is an effective sample from which to assay for biotinidase activity, but not as precise as results obtained with serum. Activity of the biotinidase enzyme may be adversely affected if the DBS specimen is mishandled. DBS specimens that are incompletely dried, exposed to moisture after drying, or exposed to heat may exhibit reduced biotinidase activity. Inconclusive or ambiguous results in screening for biotinidase deficiency are therefore often attributable to errors in sample collection and processing prior to their arrival in the screening laboratory. Another difficulty experienced in newborn screening for biotinidase deficiency involves differentiating between a complete and a partial enzyme deficiency. To aid in distinguishing between complete and partial biotinidase deficiency and subsequently increasing the sensitivity and specificity of screening for biotinidase deficiency, mutational analysis has been employed.

[0005] In the United States, the following 5 mutations are the most frequently observed in patients with biotinidase deficiency: Q456H, R538C, G98:d7i3, D444H, and the double mutation D444H:A171T. Q456H, R538C, and G98:d7i3 are associated with complete biotinidase deficiency. The D444H mutation has a carrier rate of 3.9% in the general population and causes partial enzyme deficiency. This high frequency in the general population combined with its causing a partial enzyme deficiency makes the D444H mutation similar to the Duarte D2 N314D variant in galactosemia. Interestingly, when D444H is in cis with the A171T mutation, the combined deleterious effects of both mutations result in an allele causing complete enzyme deficiency. The D444H:A171T double mutation is commonly observed in biotinidase deficient children that are ascertained by newborn screening. Using Light Cycler technology and paired hybridization probes, assays were designed to detect these 5 mutations frequently observed in biotinidase deficiency. Reported here are the assay procedures to detect these 5 commonly observed biotinidase mutations together with results from the analysis of specimens identified as presumptively positive in our prospective screening program for biotinidase deficiency. This use of mutational analysis may supplement the biochemical screening results and increases the specificity of newborn screening for biotinidase deficiency.

BRIEF DESCRIPTION OF THE DRAWINGS

[0006]FIG. 1 shows the melting curve results after analysis of the R538C biotinidase mutation.

[0007]FIG. 2 shows the melting curve results after analysis of the Q456H biotinidase mutation.

[0008]FIG. 3 shows the melting curve results after analysis of the G98:d7i3 biotinidase mutation.

[0009]FIG. 4 shows the melting curve results after analysis of the D444H biotinidase mutation.

[0010]FIG. 5 shows the melting curve results after analysis of the A171T biotinidase mutation.

SUMMARY OF THE INVENTION

[0011] The present invention relates to newborn screening for biotinidase deficiency using assays involving PCR amplification and Light Cycler platform technologies. 5 common mutations including G98:d7i3, Q456H, R538C, A171T, and D444H are now capable of being detected by a comparison of the hybrid melting temperatures with patient specimens.

[0012] Accordingly, what is provided is a method for detecting biotinidase deficiency for newborn screening, comprising amplifying a DNA strand from a specimen to thereby form an amplification product; wherein the amplification product is specific for detecting a mutation frequently observed in patients with biotinidase deficiency; allowing a pair of labeled probes to hybridize to one strand of the amplification product, wherein a detection probe is adapted to match to a sequence that may include the mutation, and an anchor probe hybridizes to an adjacent sequence, thereby forming hybrids; allowing fluorescence resonance energy transfer to occur between a donor fluorophore and an acceptor fluorophore of each hybrid, wherein an excitation wavelength of the donor fluorophore and a fluorescence of the acceptor fluorophore is acquired; and, generating a melting curve having peaks indicative of the melting temperature (Tm) of each hybrid.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

[0013] Specimens and DNA Preparation

[0014] Biotinidase deficient specimens, ascertained through either routine prospective newborn screening or high-risk screening, were retrieved from a specimen archive. Specimens retrieved from archival storage were utilized in assay development and the retrospective study. DNA was isolated from DBS specimens and 80-130 ng was utilized as template in each reaction. Specimens, characterized as homozygous for Q456H, were provided by the Department of Pediatrics, University Hospital Vienna, Vienna, Austria.

[0015] Prospective Newborn Screening for Biotinidase Deficiency

[0016] DBS specimens are submitted by hospitals. Analysis of biotinidase activity is routinely performed using the Astoria Pacific Continuous Flow Analyzer and the Astoria Pacific SPOTCHECK biotinidase enzyme assay reagents. These reagents, to assay biotinidase activity in DBS specimens, are based upon those methods described by Wolf et al. in a screening method for biotinidase deficiency in newborns, Clin. Chem. (1):125-127, 1984. Samples demonstrating biotinidase activity below the critical cut-off level of 20.0 eru (enzyme response units) are selected for genotype analysis.

[0017] Polymerase Chain Reaction and Hybridization Probes

[0018] Sequences of the human biotinidase gene (Genbank accession numbers NM00060 (SEQ. ID NO: 1), AF018630 (SEQ. ID NO: 2), AF18631 (SEQ. ID NO: 3) were the basis from which primers and probes were designed. Primer Premier 5 (Premier Biosoft, Palo Alto, Calif.) and Tm Utility 1.5 IT (Idaho Technology, Salt Lake City, Utah) software were utilized as aids to design primers for polymerase chain reaction (PCR) and hybridization probes to detect mutations. Primers and fluorescent labeled probes may also be obtained from either Operon Technology (Alameda, Calif.) or Idaho Technology (Salt Lake City, Utah). PCR reaction buffers may be obtained from Idaho Technology (Salt Lake City, Utah.). Amplification reactions utilize 1× PCR buffer, 2 mM MgCl₂, 200 μM dNTPs (Roche, Manheim, Germany), and 0.6U Klen taq (AB Peptides, St. Louis, Mo.) in a complex with TaqStart antibody (ClonTech, Palo Alto, Calif.). Preparing a complex between the polymerase and TaqStart antibody is performed according to manufacturer's instructions. The sequence of individual primers, the sequence of fluorescent hybridization probes, and the concentration at which each is used are found in Tables 1-3 as follows: TABLE 1 Assay Forward Primer conc. Seq. ID Reverse Primer conc. Seq. ID G98:d7i3 GCCCCATTACATTCCAGATTTG 0.5 4 CTCATACACGGCAGCCACAT 1.0 9 Q456H GCCCACCTTATCCAAAGAGC 0.5 5 GGTGTCGAAGCCAAGACCC 1.0 10 R538C GCTTGGCTGGGAGAATGACC 0.5 6 CTTGTAGCCTGTGGAAGTGC 1.0 11 D444H GGGGAAAGGAAGGCTATCTC 1.0 7 ACAGGTGTCGAAGCCAAGAC 0.5 12 A171T CTCCAGCGCCTGAGTTGTAT 0.13 8 TCCATTATTGCTGAACACGAC 0.25 13

[0019] TABLE 2 Assay Anchor Probe Seq. ID No. G98:d7i3 TGGTCTGCATTATGTCTGGAGCCAGAAGTA-fitc 14 Q456H TTTGATGGGCTTCACACAGTACATGGCACT-fitc 15 R538C LCred640-AGGGACTAGGAAAAGTGTGTGGTCTGTGG-P 16 D444H LCred640-AGGGCATACAGCTCTTTGGATAAGGTGGGC 17 A171T LCred640-AGGAGCCTTGTCATAGCAGTGACCCAAGGT-P 18

[0020] TABLE 3 Seq. ID Assay Detection Probe No. G98:d7i3 LCred640-GCTTGCTCTTTTCCTCTGCG-P 19 Q456H LCred640-ACTACATCCACGTGTGTGCCC-P 20 R538C CTCTATGGGCGCTTGTATGA-fitc 21 D444H TGAAGCCCATCAAAGACCCC-fitc 22 A17IT TGGTGACCAATCTTGGGACA-fitc 23

[0021] Ten microliter PCR reactions were performed in capillary tubes using a Roche Light Cycler (Manheim, Germany). Temperature cycling conditions for PCR utilizes a modified 2-step thermal cycling scheme. Specimens are ramped to 94° C. at 20°/second and held there for 0.0 seconds to denature the DNA strands. Temperature then ramps at 20°/second to 58° C. and holds at this temperature for 15 seconds at which time primers anneal and polymerization of new DNA begins. Polymerization is completed while ramping from 58° C. to 72° C. at 1.0°/second. The slow ramp speed allows polymerization to proceed, thus negating the necessity of a hold time at 72° C. Thermal cycling is repeated for 45 cycles. All amplifications are preferably performed in an asymmetric manner. Asymmetric amplifications for G98:d7i3, Q456H, R538C, and A171T assays enrich the antisense strand of the amplicon while the asymmetric amplification in the D444H assay enriches the sense strand of the amplicon. Asymmetry produces an excess of the DNA strand to which the hybridization probes will bind in the analysis phase of the assay.

[0022] Hybridization Probes and Genotyping Analysis

[0023] Genotyping is performed using paired hybridization probes, where each assay has a detection probe and an anchor probe. Probes for the G98:d7i3, Q456H, R538C, and A171T assays hybridize to the antisense strand of the amplicon while the probes for D444H assay hybridize to the sense strand of the amplicon. The detection probe hybridizes with a region of the amplicon that includes the mutation, while the anchor probe hybridizes with a region adjacent to the detection probe. When both probes are hybridized, there is a 1 base gap between the anchor and detection probes. For each set of hybridization probes, one is conjugated on the 3'end with fitc while the second is conjugated on the 5′ end with LC red640. The probe which is 5′ conjugated with LC red640 is also 3′ phosphorylated to prevent extension by taq DNA polymerase. When both probes are hybridized with the amplicon, the fluorescent moieties are brought into close proximity, and this proximity allows fluorescence resonance energy transfer to occur between the donor fluorophore (fitc) and the acceptor fluorophore (LC red640). Anchor probes have a Tm that is at least 15% higher than the corresponding detection probe, which allows the anchor probe to remain hybridized during the melting transition of the detection probe that occurs during the analysis phase of the assay.

[0024] After completing the thermal cycling program, the Light Cycler proceeds seamlessly to the analysis program. The analysis program ramps to 94° C. at 20°/second and after reaching 94° C., immediately begins to ramp at 1°/second to 35° C. Upon reaching 35° C. the temperature ramps upward at 0.1°/second to 76° C. During the entire analysis program, the excitation wavelength of fitc is provided and the fluorescence of LC red640 is continuously acquired. Melting curves are generated by plotting the fluorescence of LC red640 against temperature during the 35°-76° upward temperature ramp. Melting peaks are generated computationally by calculating the −dF/dT of the melting curve which is then plotted against temperature.

RESULT EXAMPLES

[0025] Detecting Frequently Observed Mutations in the Biotinidase Gene.

[0026]FIGS. 1-5 display analysis of individual biotinidase mutations using melting peaks generated with the Light Cycler. FIG. 1 displays the assay results for the R538C mutation and specimens that are homozygous wild type, heterozygous, and no DNA control are analyzed. No specimen that is homozygous for R538C has yet been identified. The remainder of the assays, shown in FIGS. 2-5 display specimens that are homozygous wild type, heterozygous, homozygous for the mutation, and a no DNA control. In the cases of the D444H, G98:d7i3, and R538C assays, the detection probe matches the wild type sequence. Therefore, the high temperature melting peak represents the wild type form of the gene while the low temperature melting peak represents the mutant form of the gene. In the A171T and Q456H assays, the detection probe matches the mutant form of the gene and has a 1 base pair mismatch with the wild type allele. In these assays, the high-temperature melting peak represents the mutant form of the gene while the low-temperature melting peak represents the wild type form of the gene.

[0027] Analysis of Specimens Identified through Newborn Screening as Presumptive Positive for Biotinidase Deficiency.

[0028] Through newborn screening, 49 specimens were identified as presumptively positive for biotinidase deficiency. Of these 49 specimens, 45 were suitable for genotype analysis. In the cases of the 4 specimens that were not analyzed, there was inadequate dried blood remaining on the DBS to obtain a DNA specimen. These 45 specimens were analyzed for the 5 mutations and genotyping results are shown in Table 4 as follows: TABLE 4 Genotype Spec- Based Preliminary imen Origin Allele 1 Allele 2 Diagnosis BD1 Domestic D444H/A171T D444H Partial Deficiency BD2 Domestic Q456H ND Incomplete Genotype BD3 Domestic G98:d7i3 D444H Partial Deficiency BD4 Domestic Q456H ND Incomplete Genotype BD5 Domestic ND ND — BD6 Domestic G98:d7i3 ND Incomplete Genotype BD7 Domestic Q456H ND Incomplete Genotype BD8 Domestic Q456H ND Incomplete Genotype BD9 Brazil ND ND — BD10 Domestic D444H/AI7IT R538C Complete Deficiency BD11 Turkey D444H D444H Partial Deficiency BD12 Domestic Q456H D444H Partial Deficiency BD13 Chile D444H ND Putative Partial Deficiency BD14 India G98:d7i3 G98:d7i3 Complete Deficiency BD15 Mexico D444H ND Putative Partial Deficiency BD16 Chile ND ND — BD17 Domestic ND ND — BD18 Domestic ND ND — BD19 Domestic D444H D444H Partial Deficiency BD20 Domestic Q456H ND Incomplete Genotype BD21 Domestic D444H ND Putative Partial Deficiency BD22 Brazil G98:d7i3 ND Incomplete Genotype BD23 India G98:d7i3 G98:d7i3 Complete Deficiency BD24 Domestic D444/A171T D444H/A171T Complete Deficiency BD25 Domestic D444H ND Putative Partial Deficiency BD26 Domestic Q456H D444H Partial Deficiency BD27 Domestic D444H/A171T D444H Partial Deficiency BD28 Domestic D444H D444H Partial Deficiency BD29 Domestic D444H D444H Partial Deficiency BD30 Domestic D444H D444H Partial Deficiency BD31 Domestic D444H D444H Partial Deficiency BD32 Domestic D444H ND Putative Partial Deficiency BD33 Brazil D444H D444H Partial Deficiency BD34 Domestic Q4565H ND Incomplete Genotype BD35 Domestic R538C D444H Partial Deficiency BD36 Domestic D444H ND Putative Partial Deficiency BD37 Domestic Q456H Q456H Complete Deficiency BD38 Domestic D444H:A171T ND Incomplete Genotype BD39 Domestic Q456H D444H Partial Deficiency BD40 Domestic D444H ND Putative Partial Deficiency BD41 Domestic Q456H ND Incomplete Genotype BD42 Domestic D444H ND Putative Partial Deficiency BD43 Domestic Q456H D444H Partial Deficiency BD44 Domestic R538C D444H Partial Deficiency BD45 Domestic D444H D444H Partial Deficiency

[0029] Thirty-six specimens were of domestic origin and 9 were of foreign origin (see table 4 for the countries of origin). Overall, in 88.8% (40/45) of the specimens at least 1 mutation was identified. For specimens of domestic origin, 91.6% (33/36) contained at least 1 mutation, while 78% of specimens of foreign origin (7/9) contained at least 1 mutation. A complete genotype was obtained from 21 specimens. Seventeen specimens (BD1, BD3, BD11, BD12, BD19, BD26-31, BD33, BD35, BD39, BD43-45) could be assigned a preliminary designation of partial deficiency because they were either homozygous for D444H or were compound heterozygous between D444H and one of the other mutations being assayed for. The genotypes of 5 specimens (BD10, BD14, BD23, BD24, BD37) clearly identified them as complete deficiencies, 2 of which were homozygous for G98:d7i3 (BD14, BD23), one was homozygous for D444H:A171T (BD24), one was homozygous for Q456H (BD37), and one was a compound heterozygote for D444H:A171T and R538C (BD10). Eight additional specimens (BD13, BD15, BD21, BD25, BD32, BD36, BD40, BD42) could be assigned a preliminary designation of partial deficiency owing to the presence of a single copy of the D444H mutation and reduced enzyme activity. Mutations observed in specimens of foreign origin were limited to D444H and G98:d7i3, while all 5 mutations were observed in specimens of domestic origin.

[0030] In newborn screening for biotinidase deficiency, it is frequently difficult to discern if a partial or complete enzyme deficiency has been encountered. In the vast majority of partial deficiencies, the D444H mutation is involved (8). D444H has a carrier frequency of 3.9% in the general United States population and reduces the activity of the biotinidase enzyme by 48-52%. It is noteworthy, that these percent reductions were determined with serum quantitative enzyme analysis, thus the percent enzyme reduction in a DBS derived whole blood specimen could be greater. Partial deficiencies are either homozygous for D444H or compound heterozygotes with D444H and a second mutation. In Table 2, there are seventeen specimens with genotypes identifying them as partial deficiencies. Nine specimens are compound heterozygous with D444H and a second mutation, while eight are homozygous for D444H. Additionally, there are eight other specimens where a single copy of D444H is identified. This is strong evidence that these too are partial deficiencies. It is unlikely that these eight specimens with a single copy of D444H are simple carriers because the enzyme assay was below the critical cut-off and a carrier of D444H would not be expected to produce such low enzyme activity. This suggests that such specimens are likely compound heterozygotes having one copy of D444H and a rare or private mutation in the second copy of the biotinidase gene. In the enzyme assay used in newborn screening, compound heterozygotes containing D444H and a mutation causing a complete deficiency (R538C, G98:d7i3, Q456H, etc) may generate biochemical data effectively mimicking complete biotinidase deficiency. A similar situation is frequently observed in the Beutler assay that is used to measure GALT activity when screening for galactosemia. Compound heterozygotes between the Duarte D2 N314D variant and a classical galactosemia mutation such as Q188R may generate biochemical data suggesting classical galactosemia. Identifying the N314D GALT mutation provides definitive proof that these specimens are not classical galactosemia. In a similar fashion, the D444H mutation is responsible for the vast majority of partial biotinidase deficiencies and therefore identifying this mutation provides strong evidence that a complete enzyme deficiency is not present.

[0031] A complication surrounding the D444H mutation is double mutants. Three double mutations, involving D444H and a second mutation on the same gene, have been described. The commonly observed double mutant, D444H:A171T, that accounts for 17.3% of the mutations in complete biotinidase deficiencies ascertained by newborn screening, is part of this panel. Indeed, specimen BD24 from Table 2 is homozygous for D444H:A171T. Two other double mutations, D444H:F403V and D444H:R157H, have been described, however both are extremely rare. The D444H mutation is very useful to identify partial deficiencies, but the possibility of a rare or unique double mutant resulting in a complete deficiency cannot be dismissed. After newborn screening results are reported, the first clinical visit of a potential biotinidase deficient newborn will involve determining quantitative serum biotinidase activity and possibly confirmatory molecular diagnostic analysis. Quantitative biotinidase analysis is the ultimate diagnostic test to identify biotinidase deficiency and the newborn screening analysis is secondary to these results. Second tier mutation screening is to benefit the newborn screening program and acts as a guide in clinical evaluation. However in certain situations, as are observed in specimens BD10, BD14, BD23, BD24, and BD37, the genotype data unambiguously identifies these specimens as having a complete enzyme deficiency. Such informative results can expedite patient care to get the newborn immediate attention.

[0032] The data shown in Table 4 and discussed above provides evidence to the utility of second tier mutation analysis in newborn screening for biotinidase deficiency. In a high throughput newborn screening laboratory, the most important issue is validity of results, but following closely behind is turn around time. Minimizing turn around time requires that assay platforms be fast, reliable. and easily interpreted within the context of a routine service laboratory. The Light Cycler platform is ideal for the high throughput newborn screening laboratory because all of these criteria are met. Air driven thermal cycling is fast, genotyping with fluorescent hybridization probes is simple because it involves no post-PCR manipulation, and melting peak data is easily interpreted. From isolation of DNA to data interpretation, the 5-mutation panel described here is completed in less than 2 hours. Such rapid analysis assures that second tier molecular data is reported along with the primary biochemical data. An additional benefit is that the close tube format simplifies sample tracking and is favorable for avoiding amplicon contamination in the laboratory. Data files from the Light Cycler are easily stored and may be backed up in an off-site archive rendering them safe from loss. This is an ideal situation for the newborn screening laboratory where large quantities of sensitive clinical data are generated.

[0033] In the example above, mutations that cause biotinidase deficiency were identified. Among specimens of domestic origin identified using the present methodology, the panel of five mutations proved useful in 91.6 % of presumptive positive newborns. Biochemical analysis will remain the primary means by which biotinidase deficiency is detected in both newborn screening and clinical diagnostics. Second tier mutation analysis provides valuable support to biochemical analysis and should be considered as a supplement to the biochemical data by those performing newborn screening for biotinidase deficiency.

1 23 1 2016 DNA Homo sapiens 1 gccagctgga gcgttttcgg ggctgtaaag ggagaatggc gcatgcgcat attcagggcg 60 gaaggcgcgc taagagcaga tttgtggtct gcattatgtc tggagccaga agtaagcttg 120 ctcttttcct ctgcggctgt tacgtggttg ccctgggagc ccacaccggg gaggagagcg 180 tggctgacca tcacgaggct gaatattatg tggctgccgt gtatgagcat ccatccatcc 240 tgagtctgaa ccctctggct ctcatcagcc gccaagaggc cttggagctc atgaaccaga 300 accttgacat ctatgaacag caagtgatga ctgcagccca aaaggatgta cagattatag 360 tgtttccaga agatggcatt catggattca actttacaag aacatccatt tatccatttt 420 tggacttcat gccgtctccc caggtggtca ggtggaaccc atgcctggag cctcaccgct 480 tcaatgacac agaggtgctc cagcgcctga gttgtatggc catcagggga gatatgttct 540 tggtggccaa tcttgggaca aaggagcctt gtcatagcag tgacccaagg tgcccaaaag 600 atgggagata ccagttcaac acaaatgtcg tgttcagcaa taatggaacc cttgttgacc 660 gctaccgtaa acacaacctc tactttgagg cagcattcga tgttcctctt aaagtggatc 720 tcatcacctt tgataccccc tttgctggca ggtttggcat cttcacatgc tttgatatat 780 tgttctttga ccctgccatc agagtcctca gagactacaa ggtgaagcat gttgtgtacc 840 caactgcctg gatgaaccag ctcccactct tggcagcaat tgagattcag aaagcttttg 900 ctgttgcctt tggcatcaac gttctggcag ctaatgtcca ccacccagtt ctggggatga 960 caggaagtgg catacacacc cctctggagt ccttttggta ccatgacatg gaaaatccca 1020 aaagtcacct tataattgcc caggtggcca aaaatccagt gggtctcatt ggtgcagaga 1080 atgcaacagg tgaaacggac ccatcccata gtaagttttt aaaaattttg tcaggcgatc 1140 cgtactgtga gaaggatgct caggaagtcc actgtgatga ggccaccaag tggaacgtga 1200 atgctcctcc cacatttcac tctgagatga tgtatgacaa tttcaccctg gtccctgtct 1260 ggggaaagga aggctatctc cacgtctgtt ccaatggcct ctgctgttat ttactttacg 1320 agaggcccac cttatccaaa gagctgtatg ccctgggggt ctttgatggg cttcacacag 1380 tacatggcac ttactacatc caagtgtgtg ccctggtcag gtgtgggggt cttggcttcg 1440 acacctgcgg acaggaaatc acagaggcca cggggatatt tgagtttcac ctgtggggca 1500 acttcagtac ttcctatatc tttcctttgt ttctgacctc agggatgacc ctagaagtcc 1560 ctgaccagct tggctgggag aatgaccact atttcctgag gaaaagtagg ctgtcctctg 1620 ggctggtgac ggcggctctc tatgggcgct tgtatgagag ggactaggaa aagtgtgtgg 1680 tctgtggggc ggactctggc catcatgttg acagccttgc acttccacag gctacaagcc 1740 ctgggaccat ctttctgcct taagggcagg agcccacttc tgtggcacca gattccaccc 1800 tgggaactgt ggaaaaagta ggagaggcag attccctcag tgtcttcctc ttaaacctca 1860 atcatcgaga cattaggggg tattttctgt tcacatttat ctttttcaag ccacatcttc 1920 ctctaacaaa tctctcagta tgcgattggt ctcaagctaa aacaaaaata aatgtcagtt 1980 tatattttac acatccaaaa aaaaaaaaaa aaaaaa 2016 2 1000 DNA Homo sapiens 2 cttccctccc tcccgggcgc taaaaggaaa accccccgac ccccatcgcc catttctact 60 cgtctccaag acaacatcgc ggtccccgcc agcttccgta ggagcctttc attccaggaa 120 ggtccatcgt acttgcgttt tcagggcctg agcgatgact ttagcaccag acacctgctc 180 ctcgctgcgc tctgcgaagt tactgtccgg catcttccac cgaaaagctc taagcactca 240 cgcagccggc aaacaagcgg aatcatccag caaggcaaac gcgaagtcgg cagcacgcca 300 cctctggtac tgcacctctg acggacagga gggcaaccaa ctgccttaaa caacgggaag 360 gaagaggcgg tctaaattcg tccacttccc gggagaggtg agaatgtaaa cacgcgcatt 420 ctccaatcag aactgcgctc tcttctcggc tcctccattc gcgcgccaga atgccagagg 480 gaggcgggac tagcaggaga ttgctgccta tgcaaagcag gtaagaagcc gaactctgag 540 gcctctcgcc attgtctccg agtcggccag ctggagcgtt ttcggggctg taaagggaga 600 atggcgcatg cgcatattca gggcggaagg cgcgctaaga gcaggtacgg agggggcgtg 660 gtgcggcgcg gagggggtgt ggtaagggcg tgcggtccag accccgcccc gggcgcccag 720 ttggacttgg ggagggctgc gcaaaggctg ccgggagctg ggaagcccgg cgcgcgtcgt 780 ttgctggggc tgtttgtgcg ttgctgctgt gctaccgcgt tgcgttttct aggcatttac 840 ttacacgctt tgtggtttac gctctcataa ccttgtggtt ttatagtcct taaattattg 900 tagcgcacgt tacttaaatc cagaagcaga tgtgtacccc agcaagagat aaaatgacgc 960 tcagagtcag tagatccaga ccgtgcctga gatcctgaat 1000 3 12990 DNA Homo sapiens 3 tctcactggc tgctcttatg atccagaatg gaagaggatg aggacaaatg cagggggatg 60 ttaggagacc actaagcagg tccctgtcat ttctctctct gtgattcctt ttgctgccac 120 tttctccttg tccccttggc tccagccccc tgctgtcctt gctgtttctt gcacccgccc 180 gtgaggcatg ctcctgcctc aggctctctg cctgccgtgc tctcacctcg cagacccacg 240 tgatttcctc ccgaaccccc ttcaggcctc ggtccaaaca tcaccctctc atcgaggtct 300 tccttgacca cactgcttaa aattgtcccc ctcgcctcac cttaccacct tcactgcctc 360 atttctcctt tgtgcttaat caccatctca cacagttatc cagagcacga gccccacgag 420 gaagggtctg tcttgtccac tgttggaccc ctgacaccta acccctgggg ctggcccaca 480 gttgggaatt gcatggctgt ctgaagccag caccttcctg gttctgctgt tccctggaag 540 tggggttcag tacaccccac gagccaaggc cctcatctca gagggcgtgc acatggttgc 600 ctcaattgtg ctttcacact ggacccttcc tgcagtttac tctcctatgt cagatgccct 660 tcaatgaaag caagtacatt gccaccttgt cacacctcta gttaccattt tctttatggt 720 ccaggtcctg accagctcta aagatgggtc agctgctgta tttccaagaa ccccatgact 780 tccagggccc cttgttccca ggaaggcccc gcaccccagt cgtcccgtgc ataacctcac 840 gggccagcac ctggtagctg ctggaaggct tctgggggat gcctgggccc ctccagccct 900 acctctagtc ctgccacttt acaactgagc acctcccgct gctgcctgct gaacccttca 960 gagtccttgc cacaggccct atttactttt tcctgagaag gtatgtgtga tgccaaagag 1020 agaaaagcag catttgctaa tttgggtaaa atgtttcttt gggaagggca aattgatgta 1080 cagttgtccc tcagtatctg ttgggactgg ttccaggacc ccgtggatac cgaaaccctc 1140 agatgctcaa gtcccttata tcaaatggtg tagaatttac atgtaaccta aacacttcct 1200 cctgtacact ttaaatcatc tctagatccc ttacactacc taatacaaac taaatgctat 1260 ataaataatt gttatactgt attttttaaa ttgctattat tttttattgt tgtgctatta 1320 tttttattgg gctccctcct ccccctccca ccccagtaat ttcaatccaa ggttggtgga 1380 atccatggat gcagaaacaa tggatactga gggccggctg actagaccta tttttattgt 1440 aattactcat tctcttctac ctcattaagc ttggttcttt caagcatgaa tacctggttg 1500 aatctgcata acctcttatt atcgacctac ctttgttcac acacaaatga ttgccactta 1560 gagctctcct accgggctcc ttttgtaaaa taaattttat cttctccaga tagaaagaaa 1620 tgtgatacct tgcggatttt gcggtttcct tgttttgctg gattgcaagt cctttagaca 1680 taaacaaatg ttctgtaccc cgacatcggt ggtacccagc tctcagttga gaaagagatg 1740 taatgtgaat gccactcttg gccccaggca ctcctcactt gcccccactg gggactggtt 1800 cataccctcc tctcctggcc tcagtttcca tacctcttag tgaggccttt gcgttatact 1860 tcagaaatat tgtcagtatg actttgaaga tgaaagtttg cccccaaaat cactctctgt 1920 tatcattgtg aaaccagaga tggaatggaa aaatgggttt ctgagacatt ttaaattatt 1980 ccttgcttgt ctttagaggc aaaattcaga taagaaagct tatcaattat acttttgttt 2040 ctactcaaaa actcatgact gctcactcaa agactccttg ttcttatctt aaaacattgt 2100 ttacagtgtc ccagatgaat ggcaacaaat cctggggttt ggtgtttgga tggtacattt 2160 ccctggggaa agaaataaca gtttgagatg gaacggggtt ggggtgggag aatacttctc 2220 attctgagga atatttaatt ttgccaagat gagcatttct agttcttagt ctgttgacga 2280 aaagagctat ggtttgtttc tggaactttt gataaaaaat aaagaaattt gtagcctggg 2340 gagtttggtt ttaaaatgca aacacaggag ttatgagttg agacttggac agggtgtcat 2400 tttcttttta aagggcagca atatgattct ttgatttgtc tttgttatct tgacttttaa 2460 tccggattcc tgggcagttg ttcagcccca ggacatctcc atgggcaggt ggcctggcct 2520 tggcacacta cccagtaaat ctctgcctga gaggacgctt tagctgggag gccaggctga 2580 tttttaaagg cagaattgga ctatttactc taaaacagta atgcacactg tttagaaaga 2640 aacattccta ttctgggagg aaggaggaga cacacagaag tatcatttat ttctagtctt 2700 ttctggtaga agctatgaag ctgagtttac tctctggaaa tttgtagttt attttctaga 2760 aaattgcatt ttatcactgc aaaaaggatt ttatttccaa atgagtaggc ttttgagcaa 2820 gagttttgga gtcacagaga tggggttaag aaagtgataa tgtgcaatgg cgattctcaa 2880 gttcaaggag aaaaaataac atgcttttat tgggatactt tgcttgtcta taaaagaaag 2940 tagctattgg catttatgta gaagtcagca gtttcttggc accaaataaa taattttgtg 3000 ctgaataaag ggagagttat ccatagtatt tattactaac caaagaaatg cagggagaat 3060 tgtaattcat taggttttga tggccaggaa agccaagctg tgttattagg gtcatgacaa 3120 tcacagacat tacggatggc tgacctgtag tatggataga gggcagaggg tagagtgtga 3180 aatatatcac agaattatgt caaataatct ggatagttac tactgcttaa aatctaagtg 3240 cacagctaga aaagtgggta gtgacgcact acagtcttgc tgaacactgg gtaagaaaat 3300 catagcaaac gttgagtctg ttttggaaat gttctaaaac cagactatta acacagtgag 3360 ccattttaaa tgtggcttgc tacgtgtttg gagagaaaca catactcttt tattaggaac 3420 atgaaacaaa ctctttgagc cgcagtatca ctgcgagtga gtttaattgc tgggattaat 3480 aaatcacagc tgcaaacgtt aaattcttgg caggattctt tattcagctg ttttcccctt 3540 gccccattac attccagatt tgtggtctgc attatgtctg gagccagaag taagcttgct 3600 cttttcctct gcggctgtta cgtggttgcc ctgggagccc acaccgggga ggagagcgtg 3660 gctgaccatc acgaggctga atattatgtg gctgccgtgt atgagcatcc atccatcctg 3720 agtctgaacc ctctggctct catcagccgc caagaggcct tggagctcat gaaccagaac 3780 cttgacatct atgaacagca agtgatgact gcagcccaaa aggcaagaat gctcctcgga 3840 acctgagttt ctctcataca gagcagattg ctctttaccc cttgatcagt ggttgggtaa 3900 tcccaggctt cctaccaccc tctgaaaaag catccaggta gttaacctga gttgagttag 3960 tcagttgaat taggagcctt acccctcaga gagtggtccg tggaccggca tcccctggga 4020 gcttgttaga aatacaaaat cttgggcggc accccagacc tactgaatca gaatgtgcat 4080 tgcagcagga tccccaggtg atgctttcac atggcaagta tgagaagccc aggactagat 4140 ccccagttct caagtgtggt tgtacataag aatcacgagg taagtggtaa acactatggc 4200 tgcccgggtc ctggagagtc cgttgtaatt ggtgtggaag gggtgtggac tggcactggg 4260 attgttttaa ggctccccag tgcagtctaa tgtgcagaaa aaatttgaaa gatgactggg 4320 cgtgatgacc tctctgagtc attcgaagct tcactgaagt agtaagcatc tgcaagaatg 4380 ccgtttgctc ccttcagact gtttgaggct cgtttccggt ctctatgtcg gactacgatc 4440 agtctgagac cttcgcccag atagaactga ccccaaactg acaaagggaa ggtcagtgcc 4500 agcctttgtg aaggcttcct ggttggcctg aatttcctgc tcccttcagg aagggtgggg 4560 acaaaggaga ggcccccctg ggggcaaaga gggaaatatc agaggttgcc taagaaaatg 4620 ccctgctgga aaacacaaac ccgaagggaa gtttgggctg taactctggt ggcagggtga 4680 ccaagcgcag ctgcttgagg aagccctgct gtgcctcaac aggatgtaaa ctcattgtga 4740 gcaacacttt cctgctctct gtgaacttaa agggcagaac cagcaggtcc tgccccaaac 4800 agtccctgcc ttagagcagg gtggtcggga tggcctggac agccacagca attaaaaaat 4860 tgcaacattt taaaatttta gtctataata tatatacaaa ggctatgtgt atggggtggg 4920 ggggtgtttg ggggcagggg gtgtgtatgt gtgtataaca tgatgttgaa agggaacttg 4980 aagacttggt ccagcttctt ttttttcaac caagaccaac ttttgcaagg gtgacacttt 5040 tctttagtcc caacctgaca tacggtttct ccttgaacac cttcagtggc tcagactcac 5100 aggtccgttt gttccaatgg tgggaacttc tgaacaggtc ttcctttcaa tgagcagcag 5160 tcagcctccc cgtaactgcc accacgattc tatcgtcaga gctaaaggga gcaggaccgt 5220 gtcccttatc acggcatgcc atcttctcca cctttgagga cagctgtcat gatccccctg 5280 gcatctgtcc cccaggctgt atcctcagtc ccttccacag ttccttagga gactcagttt 5340 ccaaaccttc tactgaagac ttccatgttt tctctgtgct cagaactgta tgcagctatc 5400 ccgattctgt ctaataaggg cagggtagag aactctcacc tgtcgcattc tagatgttgt 5460 ccccagaaaa ctgctggcag ccacatgtct cattatgggt gtataaggca cttgctgtca 5520 actaaaacac cttttcacat gagcagacac acatgctgcc attgccatcc tgtacttata 5580 aattataaag gtgattgatt taagctgagg gcaagacttc acatttatgc tgttaaattt 5640 catcattcca gcctgttggg ctatttaggg atctttactg acatcccaag tatcagttac 5700 ctttacgtca ttcacacata tgatacacac ctcatttatg tctatgctga agtcagtgta 5760 aaaaaacccc aggctgtgcc ctcagacctc ctgatgacac tgatctccta gagggcaggc 5820 attctcttga tagagatgtt tgcctgcatg gcactgagtc cagcacctga aatgtcatct 5880 gcctcttgct tccctcccct atccaccgga ccattctgag acatttggca aatgacacac 5940 tgaaacccag actgtggctg tagaattctc ctgcattcac ctttcaataa tctgccccca 6000 gaggaaacac ttaacacggt tttgttgaaa ccacgccagc tgcacagcat cactccgtct 6060 ctatttgttt tccaggggcc aggattaagc tgttgatatg atcactttta gaatttacag 6120 atatctcagc tcccatacgt ggttatatgt tttttatttg tttgttttcc agcagcactt 6180 ttattttcct tacacgatga catgttgctg gggcctattg ttctcacata acagtagaaa 6240 accaaaattt gttgtcatct cttcaaagaa tcgagaattg catacagaaa aaccttacat 6300 aaattaaaag gatgaataca tttacaggtg taaatgcaaa ccactttcaa ctcagacaag 6360 taacagccca tggtgttctg gcagaaaaca tcagctaaga aaggaaactg ggtcctaagt 6420 cttggacttt ccaaccctta cagaccggca gaacagaaac aactggttca ggagcccttg 6480 ccagcctcca gagaaatccc agaacacgca gccctgacgt attaataccc tgcacagatc 6540 agagactgct ggccacgcag actcaccaag ccacagactt gtcttccaca agcactttct 6600 tatcttagcc acaaagtgac caagccacat gtactaaggg ttgaaatcaa agatatgtac 6660 agggtattaa gcaaatctgg ttatatgttt taaaacaact tctaagacaa attgatggca 6720 agtttgtgtg aaagttttat atcaaagttg ttataagagg ttcctgagca aaccaattga 6780 aatacagtca tgcattgctt aatgacaggg atatgttctg aaaggatgca tcattaggcc 6840 attgtgtcat tgtgcatgca tcatagcatg tacttacaca aacctacatg gtacggccta 6900 ctatgcgcct aggctatatg gtatggccca ttgttcctag gctataaacc tttacagcat 6960 attactgtac tgaacactgt aggcagttgt aacaagtggt aagcatttgt atatgtaaac 7020 atagaaaagg tacaataaaa attcagtatt ataatcttat gggaccacca tcacatatgt 7080 ggtctgtcat tgaccaaaat gtcatcatgc agtgcatgac tatatttctg tctcagtagg 7140 ggcattcata ggggaaaaac ggagtctagt ttcaagatga ttaggctggg cagtcacttg 7200 ggattgtaac cttcattcct cagaaggaag gggttcttga tctcattgag atctaccaga 7260 aaattgctga agccatttat caagaatgca acttacttcc tagataggat tactcatcac 7320 atcagaccca aaattttgcc cagctcaggt ttggttcctc tcctcattcc tggttgataa 7380 taatctagta tgtatacata atttaaatgt tattctccat gaaaaaccaa agttttgttt 7440 ttaataaaga aaaatgtcta tccaaatata attttcaaaa atctgaaaag atgactcata 7500 caaatataga atgaataaag cttttattta attcattaat taaggaacca gtaagatggt 7560 aaagctggtt caaaggaaaa ttcaaggaat ggaaatgtgt atatcagtca gtccagtgat 7620 tgttgaaatg aatttcctaa tagatgcaaa actgggtaat gtcctatagg gcaaaacatt 7680 gtaatctttg aggtgatctt ttaaatagca aagtcaaacg gtggtacatt ctccagctaa 7740 ttaaagaata attgagtgag cctattaaac agtaccctag tataatttgg aaaggctgca 7800 tctccatctt gccttatttt taggtttgag ataatttttc tttacatggt cattgctaag 7860 tgtgcaatga gatgatactg tactggaagg aacatacatt ggtatagtat ttctggaaag 7920 cagtttggca gtgtgtgtta agaacttaaa agtttaattt ttaggccagg tgctgtggct 7980 catgcctgta atcccagcat tttgggggtc caaagcgggc ggatcacttg aggtcaggag 8040 tttgagacca gcctgatggt gaaaccccat ctccactaaa aatacaaaat ttagccaggt 8100 gtggtggcgc atgtctgtaa tcccagctac tcaggaggct gaggcacgag aattacttga 8160 acccaggagg cggagattgc agtgagccga gatcacaaca ctgcactcca gcctgggcga 8220 cagaccaaga ctctctctca aaaaacaaaa caaaaattaa aactctaatt tttataccct 8280 ttgatccagt aatttcactt gtaagacttt attccaaaga aataatcaaa agatgcaatc 8340 aaagatttgt gtgaagtgta taattatgca ataagtgttt tgagcacact atgcagatgg 8400 tcaccacagt tttcttttta ttacaaaaag ttgggaacac ttcaaattcc aataatagag 8460 gataaattat ggcgtcctct taaatatgat gtggccccat tacaaatgga tttttgaaag 8520 tttttttttt ttcctttttt ttttgtggtg gagtttcact ttgtcaccca ggctggagtg 8580 caatggtgcg atctcagctc accgcaacct ctgcctcccg ggttccagtg attctccagc 8640 ctcagcctcc tgagtagctg ggattgcagg tgcccgctac catgcctggc taatttttgt 8700 atttttagta gagacggggt ttcatcatgt tgggcaggct ggtcttgaac tcctgagctc 8760 aggtgatctg cccacctggg cctcctgaag tgctgggatt acaggcgtga actgccatgc 8820 ttggccgtat tttttaaagt tcttaatgag ggaagtcaag atgtaaaacc atatatttat 8880 tattatctcc attatataca cacatacatg tatacagaga gaaaaagtaa tgaaaataac 8940 caaaatatta acaataagta tctgtgttat agaattatga ttgttttttc ccgttttcca 9000 aattttctac agtaaaactt ttgaagcttt tataaccagg aaaaaaattt aaaagtttgc 9060 aatgcattcc agaaataagt gtctcaaact ttgctaattt gaattgttca tgccttctct 9120 gcctgccttc tccaccttcc tccctggggc tggtgttccc ggcttgacat tttaaaccct 9180 gtaagtggag agcagtggaa gaatgatgcc ccagccctga gagctgaggg cggccctgtt 9240 tgtattttct taggttgctg tagatgtcac agggagttcc gggccatcac agccagggaa 9300 cacaggatgt tgccaggtgt gggaaaaggc ctttagggtg gtcagagtcc cgaagggagc 9360 ctcctaattc ccagttgggg aatggagatt tcaagcgagt tcttgtttcc aggctgagat 9420 gagcacactt gcctcttacc cactggccca gtggatccta accttggcta caaatgagaa 9480 tcacccgggg gacctttaaa caaacactgt tgccactatc ccacccacag tcaatcaaat 9540 cagactttgt aggggtggtc ccggcatcag tggtttttca gaagttcctc aactgattta 9600 aatgcacaat ggaagttgac aaccaccaga ctgaagatac cacgtgtgtt aatgggccca 9660 atgtattcaa ggcccagtag ttggccccat ctcccctggt atcctaagaa ctctaaatcc 9720 tttctagcta ttcgcttgtc aaactcctga gcttactttc aatggagctt acacattccc 9780 tccttccctc acatgacccc aggcacagtt aatggttgtt cctagaggac tttgtctttg 9840 ttccttgggg atcaggtgga gtgagacagt atccccaaga ctaagatctc tgaggagagt 9900 aaagacacca tctctgtgcc tctggttcct gctacagagt aacttcctga tggttgccaa 9960 aagaatgaac agaagaatga atgaatgcag cggttcttcc tgccatctga taacagacta 10020 ttctttgatg ttttcatttt caggatgtac agattatagt gtttccagaa gatggcattc 10080 atggattcaa ctttacaaga acatccattt atccattttt ggacttcatg ccgtctcccc 10140 aggtggtcag gtggaaccca tgcctggagc ctcaccgctt caatgacaca gaggtgattc 10200 ctgccttttt cctcagtagg ctgagggtac acagaggtga tctaagtcag ggaccagaag 10260 ctgtgacatg ttaactaaga ttgataggag accttaacat ccccaaaatc caacccaaac 10320 tcccaaagat ccatgtgcca catgttcatt ccattaaaga atgtctgacg ttacaaggca 10380 gttattcatc tatggatctt tccatttatt aattacacaa taaatacagg aatgtatact 10440 taaaccaaac caaaagtaaa aaaagaaaag ttcatcttca ccacagcctg cacctcatcc 10500 catgcccttg cttagagaaa ctgccatcaa caatttgatg tgcattcagt tgtattcttt 10560 tctatgcatt tcatagttat tgacatcctc tttttttttt tttttttgag atggagtctt 10620 actctgccac ccaggctgga gcgcagtggc gcgatctcgg ctcactgcaa gctccgcctt 10680 ctgggttcac gccattctcc tgcctcagcc tcccgagtag ctgggactac aggcatccac 10740 caccacgccc ggctaatttt ttgtattttt agttgagatg gggtttcacc gtgttagcca 10800 gggtggtctc aatctcctga cctcatgagc cacccgcctc agcctcccac agtgctggga 10860 ttacaggcaa aaacctcatt tatttacacc tttttttcct ctaggtgctc cagcgcctga 10920 gttgtatggc catcagggga gatatgttct tggtggccaa tcttgggaca aaggagcctt 10980 gtcatagcag tgacccaagg tgcccaaaag atgggagata ccagttcaac acaaatgtcg 11040 tgttcagcaa taatggaacc cttgttgacc gctaccgtaa acacaacctc tactttgagg 11100 cagcattcga tgttcctctt aaagtggatc tcatcacctt tgataccccc tttgctggca 11160 ggtttggcat cttcacatgc tttgatatat tgttctttga ccctgccatc agagtcctca 11220 gagactacaa ggtgaagcat gttgtgtacc caactgcctg gatgaaccag ctcccactct 11280 tggcagcaat tgagattcag aaagcttttg ctgttgcctt tggcatcaac gttctggcag 11340 ctaatgtcca ccacccagtt ctggggatga caggaagtgg catacacacc cctctggagt 11400 ccttttggta ccatgacatg gaaaatccca aaagtcacct tataattgcc caggtggcca 11460 aaaatccagt gggtctcatt ggtgcagaga atgcaacagg tgaaacggac ccatcccata 11520 gtaagttttt aaaaattttg tcaggcgatc cgtactgtga gaaggatgct caggaagtcc 11580 actgtgatga ggccaccaag tggaacgtga atgctcctcc cacatttcac tctgagatga 11640 tgtatgacaa tttcaccctg gtccctgtct ggggaaagga aggctatctc cacgtctgtt 11700 ccaatggcct ctgctgttat ttactttacg agaggcccac cttatccaaa gagctgtatg 11760 ccctgggggt ctttgatggg cttcacacag tacatggcac ttactacatc caagtgtgtg 11820 ccctggtcag gtgtgggggt cttggcttcg acacctgtgg acaggaaatc acagaggcca 11880 cggggatatt tgagtttcac ctgtggggca acttcagtac ttcctatatc tttcctttgt 11940 ttctgacctc agggatgacc ctagaagtcc ctgaccagct tggctgggag aatgaccact 12000 atttcctgag gaaaagtagg ctgtcctctg ggctggtgac ggcggctctc tatgggcgct 12060 tgtatgagag ggactaggaa aagtgtgtgg tctgtggggc ggactctggc catcatgttg 12120 acagccttgc acttccacag gctacaagcc ctgggaccat ctttctgcct taagggcagg 12180 agcccacttc tgtggcacca gattccaccc tgggaactgt ggaaaaagta ggagaggcag 12240 attccctcag tgtcttcctc ttaaacctca atcatcgaga cattaggggg tattttctgt 12300 tcacatttat ctttttcaag ccacatcttc ctctaacaaa tctctcagta tgcgattggt 12360 ctcaagctaa aacaaaaata aatgtcagtt tatattttac acatccacaa agcagtggct 12420 tggggttttt tttttttttt ttatcttgtt gatcaagtga cacccaggac atgtaaatat 12480 ttcataagcc ttaaacattt cctgaggtaa gaaacaagct ctcaaagcaa aagctcaatt 12540 agaaatggcc cttgtgggga accttcccat tctggtcgac cagaactcta gccagatgaa 12600 atggcaatgc tagcgccacc agcaacgtca gaaacgtaga ccttaaagcg gttttaaaaa 12660 tagaaaagaa gcgttcctca catctgccag taatggaatt ttctgtcagt aaatggaatg 12720 tgtaggcagg acctggaata actggagaga gtgcaacgct tcggggtgaa gggcgggtgg 12780 ggactggaaa tgttgagacg ggggcagcca tgggaaggta tgagtaatag aattctttct 12840 gtacgacaca gctcatccag ggattccagg ggaccttaat aaatcacggt agctttgggc 12900 aagagttggg cacgtcgccc gactgtgcag gatggattga tgctggtatt aatttggtct 12960 ggagccctat agaggatctc gttgctttga 12990 4 22 DNA Homo sapiens 4 gccccattac attccagatt tg 22 5 20 DNA Homo sapiens 5 gcccacctta tccaaagagc 20 6 20 DNA Homo sapiens 6 gcttggctgg gagaatgacc 20 7 20 DNA Homo sapiens 7 ggggaaagga aggctatctc 20 8 20 DNA Homo sapiens 8 ctccagcgcc tgagttgtat 20 9 20 DNA Homo sapiens 9 ctcatacacg gcagccacat 20 10 19 DNA Homo sapiens 10 ggtgtcgaag ccaagaccc 19 11 20 DNA Homo sapiens 11 cttgtagcct gtggaagtgc 20 12 20 DNA Homo sapiens 12 acaggtgtcg aagccaagac 20 13 21 DNA Homo sapiens 13 tccattattg ctgaacacga c 21 14 30 DNA Homo sapiens 14 tggtctgcat tatgtctgga gccagaagta 30 15 30 DNA Homo sapiens 15 tttgatgggc ttcacacagt acatggcact 30 16 29 DNA Homo sapiens 16 agggactagg aaaagtgtgt ggtctgtgg 29 17 30 DNA Homo sapiens 17 agggcataca gctctttgga taaggtgggc 30 18 30 DNA Homo sapiens 18 aggagccttg tcatagcagt gacccaaggt 30 19 20 DNA Homo sapiens 19 gcttgctctt ttcctctgcg 20 20 21 DNA Homo sapiens 20 actacatcca cgtgtgtgcc c 21 21 20 DNA Homo sapiens 21 ctctatgggc gcttgtatga 20 22 20 DNA Homo sapiens 22 tgaagcccat caaagacccc 20 23 20 DNA Homo sapiens 23 tggtgaccaa tcttgggaca 20 

I claim:
 1. A method for detecting biotinidase deficiency for newborn screening, comprising: amplifying a DNA strand from a specimen to thereby form an amplification product; wherein said amplification product is specific for detecting a mutation frequently observed in patients with said biotinidase deficiency; allowing a pair of labeled probes to hybridize to one strand of said amplification product, wherein a detection probe is adapted to match to a sequence that may include said mutation, and an anchor probe hybridizes to an adjacent sequence, thereby forming hybrids; allowing fluorescence resonance energy transfer to occur between a donor fluorophore and an acceptor fluorophore of each said hybrid, wherein an excitation wavelength of said donor fluorophore and a fluorescence of said acceptor fluorophore is acquired; and, generating a melting curve having peaks indicative of the melting temperature (Tm) of each said hybrid.
 2. The method of claim 1, wherein said mutations are selected from the group consisting of G98:d7i3, Q456H, R538C, D444H, and A171T.
 3. The method of claim 1, wherein for the step of amplifying said DNA strand, such amplification is performed in an asymmetric manner.
 4. The method of claim 1, wherein for the step of amplifying said DNA strand, a forward primer selected from the group consisting of those such sequences as set forth in SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO 7, and SEQ ID NO: 8 is used.
 5. The method of claim 1, wherein for the step of amplifying said DNA strand, a reverse primer selected from the group consisting of those such sequences as set forth in SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO 12, and SEQ ID NO: 13 is used.
 6. The method of claim 1, wherein said detection probe is selected from the group consisting of those such sequences as set forth in SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO 21, SEQ ID NO: 22, and SEQ ID NO:
 23. 7. The method of claim 6, wherein said detection probe is conjugated with LC red640.
 8. The method of claim 7, wherein said detection probe is phosphorylated.
 9. The method of claim 6, wherein said detection probe is conjugated with fitc.
 10. The method of claim 1, wherein said anchor probe is selected from the group consisting of those such sequences as set forth in SEQ ID NO: 14, SEQ ID NO: 15, SEQ ID NO 16, SEQ ID NO: 17, and SEQ ID NO:
 18. 11. The method of claim 10, wherein said anchor probe is conjugated with LC red640.
 12. The method of claim 11, wherein said anchor probe is phosphorylated.
 13. The method of claim 10, wherein said anchor probe is conjugated with fitc.
 14. The method of claim 1, wherein for the step of generating said melting curves, said fluorescence of said acceptor fluorophore is plotted against a temperature during a 35°-76° upward temperature ramp.
 15. A method for detecting biotinidase deficiency for newborn screening, comprising: amplifying a DNA strand from a specimen to thereby form an amplification product; allowing a pair of labeled probes to hybridize to one strand of said amplification product, wherein one of said labeled probes is a detection probe selected from the group consisting of those such sequences as set forth in SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO 21, SEQ ID NO: 22, and SEQ ID NO: 23, and wherein one of said labeled probes is an anchor probe selected from the group consisting of those such sequences as set forth in SEQ ID NO: 14, SEQ ID NO: 15, SEQ ID NO 16, SEQ ID NO: 17, and SEQ ID NO: 18; thereby forming hybrids; allowing fluorescence resonance energy transfer to occur between a donor fluorophore and an acceptor fluorophore of each said hybrid, wherein an excitation wavelength of said donor fluorophore and a fluorescence of said acceptor fluorophore is acquired; and, generating a melting curve having peaks indicative of the melting temperature (Tm) of each said hybrid.
 16. The method of claim 15, wherein for the step of amplifying said DNA strand, such amplification is performed in an asymmetric manner.
 17. The method of claim 15, wherein for the step of amplifying said DNA strand, a forward primer selected from the group consisting of those such sequences as set forth in SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO 7, and SEQ ID NO: 8 is used.
 18. The method of claim 15, wherein for the step of amplifying said DNA strand, a reverse primer selected from the group consisting of those such sequences as set forth in SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO 12, and SEQ ID NO: 13 is used.
 19. The method of claim 15, wherein said detection probe is conjugated with LC red640.
 20. The method of claim 19, wherein said detection probe is phosphorylated.
 21. The method of claim 15, wherein said detection probe is conjugated with fitc.
 22. The method of claim 15, wherein said anchor probe is conjugated with LC red640.
 23. The method of claim 22, wherein said anchor probe is phosphorylated.
 24. The method of claim 15, wherein said anchor probe is conjugated with fitc. 